HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388265Generated: October 30, 2026
Hydrazine hydrate (1:1) → HCID 59185885, compound
https://huagongshe.com/reaction/388265
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 59185864 | HCID 59185864 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59185885 | HCID 59185885 | 38.8% |
Reaction Steps
To a solution of ethyl 2-(4-(dimethylamino)phenyl)-2-methoxyacetate (0.675 g, 2.84 mmol) in absolute ethanol (20 mL) was added hydrazine hydrate (0.8 mL, 16.4 mmol) and the mixture was heated at reflux for 22 hours. Additional hydrazine hydrate (1.0 mL, 20.6 mmol) was added and the heating continued for 7 hours. After cooling to room temperature, the mixture was concentrated in vacuo. The residue was dissolved in EtOAc and washed with water and brine, dried over Na2SO4 and concentrated in vacuo. The solid product was stirred with hot diethyl ether then hexanes were added. After cooling to room temperature, the solids were collected on a Büchner funnel and rinsed with 50% diethyl ether-hexanes then dried under vacuum to give 2-(4-(dimethylamino)phenyl)-2-methoxyacetohydrazide as an orange solid (0.246 g). Additional product was isolated from the mother liquor by chromatography (80-100% EtOAc-hexanes, then 5% methanol-EtOAc) to give an off-white solid (0.173 g, 66% yield total).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377930B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-372d3270dba74e39aa9f88a886192219 |
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| Source note | uspto-grants-2013_02 |
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